The [2 + 2] cycloaddition demonstrates efficient azetidines and cyclobutanes formation from alkenes, implying improved synthetic accessibility.
We report a [2 + 2] cycloaddition reaction enabled by triplet energy transfer (EnT) for the efficient construction of four-membered frameworks, including azetidines and cyclobutanes. The reaction proceeds under mild conditions with alkenes bearing biologically relevant motifs, such as 6-azauracil and coumarin, delivering products with excellent diastereo- and regioselectivity. The protocol features operational simplicity, requires no external additives, and affords the desired products in high yields with minimal side reactions.
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Mallick et al. (2025) studied this question.
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